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FDA 510(k)

MAYO CLINIC BC-10 1.5T

K-Number: K031119 · 2003-07-15

ApplicantMayo Medical Ventures
Decision Date2003-07-15
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAYO CLINIC BC-10 1.5T is the device name listed in this FDA 510(k) record. The listed applicant is Mayo Medical Ventures. It received FDA 510(k) clearance on 2003-07-15 under 510(k) number K031119. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAYO CLINIC BC-10 1.5T?

MAYO CLINIC BC-10 1.5T is a medical device that received FDA 510(k) clearance on 2003-07-15. The listed applicant is Mayo Medical Ventures. The 510(k) number is K031119.

When did MAYO CLINIC BC-10 1.5T receive FDA 510(k) clearance?

MAYO CLINIC BC-10 1.5T received FDA 510(k) clearance on 2003-07-15, under 510(k) number K031119.

Who is the listed applicant for MAYO CLINIC BC-10 1.5T?

The FDA 510(k) record lists Mayo Medical Ventures as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAYO CLINIC BC-10 1.5T?

The FDA product code for MAYO CLINIC BC-10 1.5T is MOS.

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Related Devices (Code: MOS)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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